FIELD: pharmacology.
SUBSTANCE: invention relates to compound of formula (IV) or to pharmaceutically acceptable salt thereof, wherein R1 is selected from C1-6alkyl, optionally substituted with hydroxy or methoxy, and tetrahydropyran; R2 is a hydrogen atom; R3 is -C(O) OC1-6alkyl; R4 is methyl, methoxy or -CH2OCH3; R7 is selected from atom of fluoro, chloro, -CF3 and -OCF3; R8 independently represents methyl or hydroxymethyl; R9 is selected from -NHCH3, cyclopropyl, 2.2-dimethylcyclopropyl, tert-butyl, C1-6alkyl substituted with -OH, and imidazolyl; R10 is hydrogen atom or hydroxymethyl; a takes on a value of 1 or 2; and b takes on a value of 1 or 2. The invention also relates to heterocyclic compound of formula (V), specific compound, pharmaceutical composition based on compound of formulas (IV) or (V), method for preparing a target compound, intermediate compound, as well as to application of the produced compounds and method for inhibiting hepatitis C virus replication.
EFFECT: new heterocyclic compounds are obtained, useful in the treatment of a viral infection of hepatitis C virus.
15 cl, 1 dwg, 29 tbl, 24 ex
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Authors
Dates
2017-07-19—Published
2012-11-02—Filed